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Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

ABCG2 protein marks stem-like skin cells in human epidermis.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Overactive Stat3 in mouse skin causes hair loss and cell structure damage.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Steroid sulfatase inhibitors could help treat hormone-related disorders and cancers.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

TGase 3 helps build hair structure by forming strong bonds between proteins.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Sp6 promotes tooth development by reducing follistatin levels.

Wnt1a from stem cells boosts hair growth and regeneration in mice.

Somatostatin helps hair follicles suppress immune responses, which might aid in treating certain hair loss conditions.

FGF13 gene changes cause excessive hair growth in a rare condition.

New compounds were found to help increase hair growth and decrease hair loss.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Angiopoietin-1 helps hair follicle cells survive and grow, potentially treating hair loss.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

Higher TGF-β signaling may increase skin cancer risk in organ transplant recipients.

MPA increases cancer spread by boosting Eph A2 activity.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

A pathway helps maintain long telomeres in both stem and cancer cells.